At Cernais, we believe that happy, healthy people do the best science.We promote remote work, a shorter workweek, time with family, and space for sport and self-care.Because taking care of yourself isnāt optional ā itās essential. š #WorkCulture#Wellbeing#Biotech
Please join the XLID98 Foundation on May 31, 2025 for their first conference for the #XLID98 community. This virtual event is an opportunity to hear from medical professionals, therapists, and other parents about the research, challenges, and successes surrounding this geneticā¦
CERNAIS is offering a paid internship for a graduate student with strong IT skills.Weāre especially looking for candidates with solid knowledge of Python and R.
#Internship#Biotech#Python#RStats#CERNAIS#Hiring
Today in Italy we celebrate Motherās Day.
Happy Motherās Day to all the incredible mums around the world! Buona festa della Mamma da tutti noi di CERNAIS! š§¬#MothersDay#FestaDellaMamma#CERNAIS#Biotech
Happy Labour Day from CERNAIS! Buona Festa dei Lavoratori da CERNAIS! Oggi celebriamo lāimpegno, lāinnovazione e la passione che guidano la nostra ricerca verso un futuro senza malattie rare. š§¬š¬
#FestaDeiLavoratori#Biotech#CERNAIS
Cernais is committed to improving the lives of individuals and families living with autism. Together, we can raise awareness, foster understanding, and create a more inclusive world. #AutismAwarenessDay#CernaisCares#InclusionMatters
Please read our new blog regarding advances in Rett syndrome treatments and our contribution towards the ambitious goal of finding a cure for this and many other serious X-linked disorders. #rare_disease#small_molecules#curecernais.com/exploring-advaā¦
CERNAIS is happy to announce a collaboration with Uncommon Therapeutics for the development of a new combo treatment for Rett syndrome. hashtag#AI hashtag#rare_diseases hashtag#Rett_syndrome
Last week, we officially registered CERNAIS SRL, an AI-powered drug discovery company, and today, we won the "Best Tuscany Start-Up 2024" competition. Congratulations to the entire team! youtube.com/watch?v=KOoqwjā¦#AI#rare_disease
2K Followers 919 FollowingAlso @[email protected] RNA molecular biology & RNA therapeutics lab at the Houston Methodist Research Institute. Views =/= those of Houston Methodist
1K Followers 1K FollowingA 501(c)(3) advocacy organization dedicated to globally raising awareness of the rare neuromuscular diseases known as Limb-girdle muscular dystrophy (LGMD).
72K Followers 41K FollowingI am a professional Graphics designer. I specialize pencil portrait, logo design 3D animation video Business Card design contact Me š±š·š±š·
2K Followers 25 FollowingWe love all things RNA! We from @ericmiskalab run a monthly seminar series on topics related to RNA biology and chemistry. Sponsored by @RNAsociety and @lexogen
1K Followers 378 Followingepilepsy, neurodevelopmental disorders, genetics š§ š§¬ | #innovation for #RareDisease | champion of red wine and nacho connoisseur | opinions are mine
4K Followers 1K FollowingThe Center for RNA Biomedicine brings together researchers from multiple medical & scientific fields to better understand the role of human genetics in disease.
7K Followers 535 FollowingThe official journal of the RNA Society. Featuring cutting edge research in RNA Biology, biochemistry, genetics, cell biology, structural biology and genomics
5K Followers 1K FollowingRNA Therapeutics Institute @UMassChan; Uniting nucleic acid scientists w/clinicians to devise human therapies. Loving RNA before it was cool. #RNATx2025
88 Followers 170 FollowingRare Disease 360Ā® is an all-encompassing resource hub that compiles the entirety of relevant information on multiple rare disease states.
16K Followers 30 FollowingOfficial account of the RNA Society; on a mission for an RNA emoji; often enjoys base-pairing; always a fan of U.
Bluesky: @rnasociety.bsky.social
2K Followers 153 Following#RNA loves company. Unconventional RNA-binding proteins. The iron is still hot. Old games. New players. #Research group @embl.
312 Followers 295 FollowingSocietĆ di consulenza, offre supporto ad imprese ed enti nei processi di ricerca ed innovazione. Ć parte del gruppo #PNO con 400 consulenti in 9 Paesi Europei.
4K Followers 528 FollowingNon-Coding RNA (ISSN 2311-553X) is an #openaccess journal on #ncRNA and their regulatory roles. @MDPIopenaccess. Indexed in ESCI, BIOSIS Previews and Scopus.
5K Followers 1K FollowingThe Centro Nacional de AnĆ”lisis Genómico carries out projects in genome analysis to improve peopleās health and quality of life
#genomics #personalisedmedicine
790 Followers 54 FollowingAn interdisciplinary lab that brings together concepts from chemistry, physics, and medicine to understand protein misfolding and self-assembly. @ChemCambridge
595 Followers 152 FollowingWe're Gian Gaetano Tartaglia at IIT working on protein-RNA interactions & phase separation. We love diversity and creativity and strive for excellence.
482K Followers 2K FollowingCo-host NEXT LEVEL CHEF on FOX. I create restaurant concepts. I perform and speak on stage, in front of cameras and microphonesā¦
562 Followers 540 FollowingWe are a 501(c)(3) tax exempt public charity. Our goal is to fund cutting-edge research to find a cure for the genetic disease SLC13A5 Epilepsy.
175 Followers 524 FollowingRareRising, is a 501c3 that delivers research, incubates emerging rare disease entities, and explores solutions to positively impact rare disease communities.
294 Followers 485 FollowingOur mission is to improve the lives of those affected by Lafora disease and help accelerate the development of treatments.
Find us: @chelseashopelaforacure
3K Followers 1K FollowingWe are dedicated to improving the lives of children and adults living with Dravet Syndrome, a rare epilepsy, through medical research, education and support.
5K Followers 318 FollowingA feed for the blog https://t.co/pXYAKACULR. Discusses the covalent modification of proteins. Available on bsky and mass std don
3K Followers 1K Followingš§ š§¬ Neuroscientist. Looking for new medicines for CDKL5, SCN1A, SHANK3, DHPS and a few others. @cnsdrughunter.bsky.social
951 Followers 336 FollowingNon-profit dedicated to ending STXBP1-related disorders, rare neurodevelopmental and epileptic encephalopathies, and spreading awareness of this rare disease.
2K Followers 617 FollowingRare Epilepsy Network (REN) is working with urgency to collaboratively improve outcomes of rare epilepsy patients & families via research and advocacy.
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